HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1390602Generated: November 4, 2026
Hydrochloric Acid → 2,4-Dichloro-alpha-(chloromethyl)benzenepropanol
https://huagongshe.com/reaction/1390602
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 2,4-Dichlorobenzyl chloride | HCID 7212 | — |
| Reactant | Epichlorohydrin | HCID 7835 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2,4-Dichloro-alpha-(chloromethyl)benzenepropanol | HCID 20476872 | — |
Reaction Steps
To a stirred and refluxing Grignard-complex, previously prepared starting from 98 parts of 1-(chloromethyl)-2,4-dichlorobenzene and 14 parts of magnesium in 70 parts of 1,1-oxybisethane, is added dropwise a solution of 46.5 parts of 2-(chloromethyl)oxirane in 350 parts of 1,1'-oxybisethane. Upon completion, stirring at reflux temperature is continued overnight. The reaction mixture is cooled in an ice-bath and decomposed by dropwise addition of 120 parts of a concentrated hydrochloric acid solution. The whole is poured onto water and the layers are separated. The organic phase is washed three times with water. The aqueous phase is extracted with 1,1'-oxybisethane. The combined organic phases are dried, filtered and evaporated. The residue is distilled, yielding 2,4-dichloro-α-(chloromethyl)benzenepropanol; bp. 130° C. at 0.04 mm. pressure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04139540 |
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| Source dataset | uspto-grants-1979_02 |
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| ORD ID | ord-a7550d53dba14c3a9ad28f6a35d02bba |
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| Source note | uspto-grants-1979_02 |
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